Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome

Introduction: Rubinstein-Taybi syndrome (RSTS) is a rare congenital disorder characterized by developmental and intellectual disability, broadening of thumbs and halluces, and characteristic facial features. Pathogenic variants in CREBBP lead to RSTS type 1 (RSTS1) and in EP300 lead to RSTS type 2 (RSTS2). Individuals with RSTS can demonstrate a variety of behavioral and neuropsychiatric challenges, including anxiety, hyperactivity/inattention, self-injury, repetitive behaviors, and aggression. Behavioral challenges are consistently reported as one of the primary factors impacting quality of life. Despite the high prevalence and morbidity of behavioral and neuropsychiatric features of RSTS, a paucity of data exists regarding its natural history. Methods: To better understand the neurocognitive and behavioral challenges faced by individuals with RSTS, 71 caregivers of individuals with RSTS, ranging in age from one to 61 years, completed four questionnaires measuring obsessive compulsive disorder (OCD)-like symptoms, anxiety, challenging behaviors, and adaptive behavior and living skills. Results: Results revealed a high prevalence of neuropsychiatric and behavioral challenges across ages. We found specific challenging behaviors were worse in school age individuals. Scaled adaptive behavior and living skill scores differed across ages with an increased gap between typically developing peers becoming more apparent at older ages. Between types, individuals with RSTS2 had better adaptive behavior and living skills and less stereotypic behaviors but higher social phobia than individuals with RSTS1. Further, female individuals with RSTS1 appear to have increased hyperactivity. However, both groups had impairments in adaptive functioning compared to typically developing peers. Discussion: Our findings support and expand previous reports of a high prevalence of neuropsychiatric and behavioral challenges in individuals with RSTS. However, we are the first to report differences between types of RSTS. Further, age-related differences were seen with higher challenging behaviors within school-age individuals, which may improve over time, and lower adaptive behavioral skills compared to normative scales. Anticipation of these potential differential challenges across age is vital for proactive management for individuals with RSTS. Our study underscores the importance of enacting neuropsychiatric and behavioral screening earlier in childhood so appropriate management can be implemented. However, further longitudinal studies in larger cohorts are needed to understand better how behavioral and neuropsychiatric characteristics of RSTS evolve over the lifespan and differentially affect subpopulation groups.

[1]  L. Schmitt,et al.  Systematic Review: Emotion Dysregulation in Syndromic Causes of Intellectual and Developmental Disabilities. , 2022, Journal of the American Academy of Child and Adolescent Psychiatry.

[2]  G. Michelini,et al.  Age-related hallmarks of psychopathology in Cornelia de Lange and Rubinstein-Taybi syndromes. , 2022, Research in developmental disabilities.

[3]  R. Hennekam,et al.  The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience , 2022, European Journal of Human Genetics.

[4]  C. Barthélémy,et al.  A comparative study of cognitive and socio-emotional development in children with Rubinstein-Taybi syndrome and children with Autism Spectrum Disorder associated with a severe intellectual disability, and in young typically developing children with matched developmental ages. , 2021, Research in developmental disabilities.

[5]  L. Lynd,et al.  Out‐of‐pocket and private pay in clinical genetic testing: A scoping review , 2021, Clinical genetics.

[6]  E. Zackai,et al.  EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients , 2020, American journal of medical genetics. Part A.

[7]  V. Faundes,et al.  FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome , 2020, Scientific Reports.

[8]  I. Apperly,et al.  An Observational Study of Social Interaction Skills and Behaviors in Cornelia de Lange, Fragile X and Rubinstein-Taybi Syndromes , 2020, Journal of autism and developmental disorders.

[9]  Z. Al-Hassnan,et al.  Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report , 2019, BMC Medical Genetics.

[10]  S. Avignone,et al.  Rubinstein–Taybi syndrome: New neuroradiological and neuropsychiatric insights from a multidisciplinary approach , 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[11]  C. Oliver,et al.  Diverse Profiles of Anxiety Related Disorders in Fragile X, Cornelia de Lange and Rubinstein–Taybi Syndromes , 2017, Journal of autism and developmental disorders.

[12]  B. D. de Vries,et al.  Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by EP300 mutations , 2016, American journal of medical genetics. Part A.

[13]  J. Moss,et al.  A Comparative Study of Sociability in Angelman, Cornelia de Lange, Fragile X, Down and Rubinstein Taybi Syndromes and Autism Spectrum Disorder. , 2016, American journal on intellectual and developmental disabilities.

[14]  G. Scarano,et al.  Insights into genotype–phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein–Taybi syndrome patients , 2015, Clinical genetics.

[15]  A. Nordgren,et al.  CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome , 2015, Molecular genetics & genomic medicine.

[16]  J. Moss,et al.  Repetitive Behavior in Rubinstein–Taybi Syndrome: Parallels with Autism Spectrum Phenomenology , 2015, Journal of autism and developmental disorders.

[17]  G. Scarano,et al.  Clinical and molecular characterization of Rubinstein‐Taybi syndrome patients carrying distinct novel mutations of the EP300 gene , 2015, Clinical genetics.

[18]  W. Goodman,et al.  Obsessive-compulsive disorder. , 2014, The Psychiatric clinics of North America.

[19]  L. Curfs,et al.  Elimination disorders in persons with Prader–Willi and Fragile‐X syndromes , 2013, Neurourology and urodynamics.

[20]  M. D. Graf,et al.  Genetic testing insurance coverage trends: a review of publicly available policies from the largest US payers. , 2013, Personalized medicine.

[21]  M. Keshavan,et al.  A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome. , 2013, Research in developmental disabilities.

[22]  R. Kosaki,et al.  Age‐dependent change in behavioral feature in Rubinstein‐Taybi syndrome , 2012, Congenital anomalies.

[23]  Donna B. Pincus,et al.  Sleep-Related Problems in Children and Adolescents With Anxiety Disorders , 2011, Behavioral sleep medicine.

[24]  C. Stevens,et al.  Adults with Rubinstein–Taybi syndrome , 2011, American journal of medical genetics. Part A.

[25]  S. Tuinier,et al.  Psychiatric Profile in Rubinstein-Taybi Syndrome , 2009, Psychopathology.

[26]  M. Bouvard,et al.  Socio-Behavioral Characteristics of Children with Rubinstein-Taybi Syndrome , 2009, Journal of autism and developmental disorders.

[27]  S. Whiteside,et al.  Exploring the utility of the Spence Children's Anxiety Scales parent- and child-report forms in a North American sample. , 2008, Journal of anxiety disorders.

[28]  J. Carr Stability and change in cognitive ability over the life span: a comparison of populations with and without Down's syndrome. , 2005, Journal of intellectual disability research : JIDR.

[29]  E. Seemanová,et al.  DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein–Taybi syndrome (RSTS) and in another patient with incomplete RSTS , 2005, Human Genetics.

[30]  J. Carey,et al.  Rubinstein-Taybi syndrome: a natural history study. , 2005, American journal of medical genetics. Supplement.

[31]  Olga V. Demler,et al.  Lifetime prevalence and age-of-onset distributions of DSM-IV disorders in the National Comorbidity Survey Replication. , 2005, Archives of general psychiatry.

[32]  Johan T den Dunnen,et al.  Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease. , 2005, American journal of human genetics.

[33]  R. Rapee,et al.  A parent-report measure of children's anxiety: psychometric properties and comparison with child-report in a clinic and normal sample. , 2004, Behaviour research and therapy.

[34]  C. Stevens,et al.  Rubinstein‐Taybi syndrome medical guidelines , 2003, American journal of medical genetics. Part A.

[35]  C. Cruaud,et al.  Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome , 2002, Journal of medical genetics.

[36]  G. Fisch,et al.  Longitudinal Changes in Cognitive and Adaptive Behavior Scores in Children and Adolescents with the Fragile X Mutation or Autism , 2002, Journal of autism and developmental disorders.

[37]  Avi Sadeh,et al.  Sleep, neurobehavioral functioning, and behavior problems in school-age children. , 2002, Child development.

[38]  C. Reid,et al.  Rubinstein-Taybi syndrome and psychiatric disorders. , 2002, Journal of intellectual disability research : JIDR.

[39]  T. Achenbach,et al.  The Child Behavior Checklist and related forms for assessing behavioral/emotional problems and competencies. , 2000, Pediatrics in review.

[40]  H. Boer,et al.  Development and Behaviour in Genetic Syndromes: Rubinstein‐Taybi Syndrome , 1999 .

[41]  M. Weissman Cross-National Epidemiology of Obsessive-Compulsive Disorder , 1998, CNS Spectrums.

[42]  B. Howard,et al.  The Transcriptional Coactivators p300 and CBP Are Histone Acetyltransferases , 1996, Cell.

[43]  Raoul C. M. Hennekam,et al.  Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP , 1995, Nature.

[44]  Y. Makita,et al.  Submicroscopic deletion of chromosome region 16p13.3 in a Japanese patient with Rubinstein-Taybi syndrome. , 1994, American journal of medical genetics.

[45]  K. Jackson,et al.  Frequency of obsessive-compulsive disorder in a community sample of young adolescents. , 1994, Journal of the American Academy of Child and Adolescent Psychiatry.

[46]  M. Weissman,et al.  The cross national epidemiology of obsessive compulsive disorder. The Cross National Collaborative Group. , 1994, The Journal of clinical psychiatry.

[47]  E. Mariman,et al.  Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3. , 1993, American journal of human genetics.

[48]  W. Goodman,et al.  Assessment of severity and change in obsessive compulsive disorder. , 1992, The Psychiatric clinics of North America.

[49]  N. Tommerup,et al.  Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3). , 1992, American journal of medical genetics.

[50]  D. Lacombe,et al.  Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3. , 1992, American journal of medical genetics.

[51]  Y. Kuroki,et al.  Rubinstein-Taybi syndrome with de novo reciprocal translocation t(2;16)(p13.3;p13.3). , 1991, American journal of medical genetics.

[52]  M. Aman,et al.  Psychometric characteristics of the aberrant behavior checklist. , 1985, American journal of mental deficiency.

[53]  J H RUBINSTEIN,et al.  Broad thumbs and toes and facial abnormalities. A possible mental retardation syndrome. , 1963, American journal of diseases of children.

[54]  A. Reiss,et al.  The Influence of Hyperactivity, Impulsivity, and Attention Problems on Social Functioning in Adolescents and Young Adults With Fragile X Syndrome , 2019, Journal of attention disorders.

[55]  J. Espada,et al.  Spence Children’s Anxiety Scale--Parent Version; Spanish Translation , 2019, PsycTESTS Dataset.

[56]  M. Aman,et al.  Validity of the Aberrant Behavior Checklist in Children with Autism Spectrum Disorder , 2014, Journal of autism and developmental disorders.

[57]  S. Havercamp,et al.  Factor analysis and norms for parent ratings on the Aberrant Behavior Checklist-Community for young people in special education. , 2002, Research in developmental disabilities.

[58]  W. Liemohn,et al.  Behavioral characteristics of three children with the broad thumb-hallux (Rubinstein-Taybi) syndrome. , 1977, Biological psychiatry.

[59]  C. Oancea,et al.  [The Rubinstein-Taybi syndrome]. , 1971, Neurologia, psihiatria, neurochirurgia.